Takatsuka Ayumu, Kazama Tomohiko, Arimura Shin-Ichi, Toriyama Kinya
Laboratory of Environmental Biotechnology, Graduate School of Agricultural Science, Tohoku University, 468-1 Aramaki Aza Aoba, Aoba-ku, Sendai, Miyagi, 980-8572, Japan.
Laboratory of Genome Chemistry and Engineering, Graduate School of Agriculture, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.
Plant J. 2022 May;110(4):994-1004. doi: 10.1111/tpj.15715. Epub 2022 Mar 10.
Cytoplasmic male sterility (CMS) is a trait that causes pollen or anther dysfunctions, resulting in the lack of seed setting. CMS is considered to be caused by the expression of a unique mitochondrial open reading frame referred to as CMS-associated gene. orf312 has been reported as a CMS-associated gene of Tadukan-type CMS (TAA) in rice (Oryza sativa L.), which exhibits impaired anther dehiscence; however, evidence thereof has not yet been reported. Here, we took a loss-of-function approach, using a mitochondria-targeted transcription activator-like effector nuclease (mitoTALEN) designed to knock out orf312 in TAA, to prove that orf312 indeed is a CMS-causative gene. Out of 28 transgenic TAA plants harboring the mitoTALEN expression vector, deletion of orf312 was detected in 24 plants by PCR, Southern blot, and sequencing analyses. The 24 plants were grouped into three groups based on the deleted regions. All orf312-depleted TAA plants exhibited recovery of anther dehiscence and seed setting. The depletion of orf312 and fertility restoration was maintained in the next generation, even in mitoTALEN expression cassette null segregants. In contrast, orf312-retaining plants were sterile. These results provide robust evidence that orf312 is a Tadukan-type CMS-causative gene.
细胞质雄性不育(CMS)是一种导致花粉或花药功能异常,从而导致无法结实的性状。CMS被认为是由一个独特的线粒体开放阅读框(称为CMS相关基因)的表达引起的。orf312已被报道为水稻(Oryza sativa L.)中田都kan型CMS(TAA)的一个CMS相关基因,该类型表现出花药开裂受损;然而,尚未有相关证据报道。在这里,我们采用功能缺失方法,使用一种靶向线粒体的转录激活样效应核酸酶(mitoTALEN),旨在敲除TAA中的orf312,以证明orf312确实是一个导致CMS的基因。在28株携带mitoTALEN表达载体的转基因TAA植株中,通过PCR、Southern杂交和测序分析,在24株植株中检测到orf312的缺失。根据缺失区域,将这24株植株分为三组。所有缺失orf312的TAA植株都表现出花药开裂和结实恢复。即使在mitoTALEN表达盒无效分离株中,orf312的缺失和育性恢复在下一代中也得以维持。相比之下,保留orf312的植株是不育的。这些结果提供了有力证据,证明orf312是田都kan型CMS的致病基因。